Tag | Content |
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EnhancerAtlas ID | HS136-08713 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:79702240-79703500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr17:79703254-79703264 | GGGGCGGGGC | - | 6.02 | NFE2L1 | MA0089.2 | chr17:79702644-79702659 | CCTGCTGAGTCACGC | - | 6.2 | Nfe2l2 | MA0150.2 | chr17:79702646-79702661 | TGCTGAGTCACGCGC | - | 6.12 | TCFL5 | MA0632.2 | chr17:79702653-79702663 | TCACGCGCAC | + | 6.02 | ZNF263 | MA0528.1 | chr17:79702828-79702849 | CCCACTTCCCCTTCCTTCTCC | - | 7.03 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24622 | chr17:79702312-79703531 | Colon_Crypt_2 | SE_24986 | chr17:79700763-79703622 | Colon_Crypt_3 | SE_27510 | chr17:79702120-79703723 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081735 | chr17 | 79702231 | 79703548 |
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Enhancer Sequence | GGAGCAACAC CGATGCCACA CCTGGCGGCA GGAACAGGGC AGTGATGGGC TGTCTGCAAG 60 GGGTCCCCCC TTCCGCAGCA GGTCTCTTGG CTGCAGCTCA GCCCCAGCCC CTGCGGTCCC 120 CAGAGTCCCG GTCACTGGGG GCTCTGCAGG CCACCCTTCC AGGGGCATCC ACCCACCCCC 180 GAGTCCGGGT CAGGCAGAAC CCAGGGCCCG CCGTCCCCTC CTGCAGGCTC AGGACCTCCT 240 GGGGGGAGTT CCCTGTGTGA TGCAGAGGGC ACGCTCACCC TGCTGGGAAG GCTCACTGCT 300 TCCCAAGGGG TCTGAGCTTT ACTGGCACCT CACTGCAGTC CCTTCCCCGG GGAGACTCTG 360 GGGCTTCCCC TGTGGGACCA GGCACCCGGA AAGGCAGCTC TGTCCCTGCT GAGTCACGCG 420 CACCATCCTG CAGACGGGAG GGCATCTTCC TAGGCTTTCC TCCAGCCAAG AGTGGAGCTG 480 GGACCTGGGA ACCTCCCTGG AACCACCCCT GCTCTCCGGC AAGGCGTTCC ACCAGCCTGT 540 GTCTACACAC GTAGCCCCGC AGAGCAGGCT TCGTGATGCC TGGAGACACC CACTTCCCCT 600 TCCTTCTCCT GGGACTTCTC AGTCACACGG GCTGAGCTGC AGAGGGTGCG TGACCTGGGC 660 TGAGCTGGTC TTTGGCAACT GGGGACTTTG GTTTGACGGT TGGTGGAGGG GAGACTCTCC 720 TAACTTCCAG GGGTGTGAGT CGCAGGCGGT GCAGATGATA GGACAGTGGC CGTTGCCTAG 780 GGCTGAAACC AACACAGCGG TGGGCGGAGC ACAGGGAACT TCGGAGAGGG AGCCCGGCCC 840 CCGAGTCAGC TGCTCCTGCG GGTGCTCCCC AAATCATCTA GTGATGTGAT CCATTTGTCT 900 TTCCAGCCCA TTTCAGTTGA GTTTCCAATG ACTTACAACC AATAATATCT CAACTGATAC 960 TTGGGCTCTT CAAGCACTAG AATTGTGGTG ACGGCAGGAG CGTTAACACA CTCTGGGGCG 1020 GGGCAGGGAC TGCAGACTGA GCGGGCTCCA GGTGAATGCC AGCTTCCAGC CCTGCTGAGC 1080 CAGGCTGGGA CGAACATGCT CACTAGGTCC GTCTCCACCT ACTGTGGGCC AGCGCTGCGT 1140 GGCTCACTCC AGGGAAGACA GCAAGTTGGC TCAGCCGCTG CTGTGTGGCT GCTGCTCCCC 1200 TGAGTTTATG GCTGTCCATG GCATCTGCCA GGGTCCATCT GGTTTTTTGT GGGAATTGTG 1260
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